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Sexuality and Reproductive Issues (PDQ®)
Patient VersionHealth Professional VersionEn españolLast Modified: 08/20/2008



Purpose of This PDQ Summary






The Prevalence and Types of Sexual Dysfunction in People With Cancer






Factors Affecting Sexual Function in People With Cancer






Assessment of Sexual Function in People With Cancer






Pharmacological Effects of Supportive Care Medications on Sexual Function







Treatment of Sexual Problems in People With Cancer






Fertility Issues






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Changes to This Summary (08/20/2008)






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Treatment of Sexual Problems in People With Cancer

Although research is beginning to clarify the frequency and types of sexual problems people with cancer experience, few treatment programs for sexual dysfunction in cancer patients have been designed or tested. Programs that integrate medical and psychological modalities aimed at the treatment of sexual dysfunction in those who have had cancer are warranted. Additionally, these programs must be cost-effective and accessible to people with cancer.

Many patients are fearful or anxious of their first sexual experience after treatment and can often begin a pattern of sexual avoidance. If the patient is concerned about sending mixed signals to his or her partner, this can lead to avoidance of general intimacy and touch. The partner may also contribute to the generalized avoidance of intimacy through his or her reluctance to initiate any behavior that may be perceived as pressure to be more intimate or may contribute to any potential physical discomfort from greater expression of physical intimacy. Providers need to reassure patients and their significant others that even when intercourse is difficult or impossible, their sex lives are not over. The couple can give and receive pleasure and satisfaction by expressing their love and intimacy with their hands, mouths, tongues, and lips. Providers should encourage the couple to express affection in alternative ways (e.g., hugging, kissing, nongenital touching) until they feel ready to resume sexual activity. The couple should be encouraged to communicate honest feelings, concerns, and preferences.

If a man cannot attain an erection firm enough for penetration, and/or if intercourse is painful for a woman, some couples may be willing to find alternative ways to bring each other to orgasm and express sexual intimacy. Sensate focus exercises of noncoital pleasuring,[1,2] based on principles of sensuous massage, give couples an experience of sexual expression that allows them to be physically close and intimate without pressure and anxiety that can be associated with anticipation of intercourse. The structure and ground rules of sensate focus can help bypass performance anxiety (self-consciousness and self-evaluation) and enable the couple to lose themselves in the current experience of pleasurable touch. These exercises also help the couple communicate about potentially problematic or emotionally sensitive areas of the body. Providers should determine a couple’s openness to modification of their sexual technique.

As many patients will experience anticipatory anxiety about re-establishing sexual intimacy with their partner and potential uncertainty of their own sexual response, the potential advantages of self-stimulation can be explored. Self-stimulation has the advantage of allowing the individual to become comfortable with his/her sexual response and arousal without the added pressure of performance anxiety commonly heightened by concern for their partner’s pleasure, reactions, concerns, and/or fears. For many individuals, a cognitive reframing of masturbation to self-stimulation or self-pleasuring allows the individual to accept this activity as part of the process in sexual rehabilitation. For others, this behavior may still be a resilient and persistent taboo for cultural and religious reasons.

For those couples who wish to have sexual intercourse, sexual positions that place no weight on a scar or ostomy and positions that allow better control of depth of penetration can be explored. The side-by-side position (spooning) in which the man is behind the woman, or the L-shaped position, with both partners lying down, torsos at right angles and legs entwined, are two possibilities. Comprehensive pamphlets on sexuality and cancer, for both men [3] and women,[4] provide illustrations of sexual positions and other self-help information.

For patients with colostomies or ileostomies, pamphlets are available from national organizations related to resuming sexual activity including topics such as sex and the female ostomate, sex and the male ostomate, and gay and lesbian ostomates. Providers can educate patients on limiting food intake before anticipated sexual activity, watching the types of food consumed, and planning times for intimacy when a bowel movement is less likely. Although the ostomy pouch is typically changed when about one-third full, patients should be taught to empty the pouch sooner when anticipating sexual intimacy. Patients may fear that the ostomy bag will interfere with sexual intimacy, become dislodged, or cause damage to the stoma. An empty and flat ostomy bag will not become dislodged from the stoma and can be rolled up or taped down so that it will not get in the way of sexual intimacy. Decorative covers may also be worn.[5,6] A much greater selection of products for ostomates exists today than in years past, including disposable pouches, reusable pouches that empty from the bottom or top while still attached, pouches with filters to control odors, and pouches that hang sideways instead of down for physical activity. Patients concerned about potential odor can use deodorant tablets or liquids in the bottom of the pouch or as recommended by the manufacturer.[6]

Providers can help educate couples by offering practical suggestions to overcome changes in responsiveness to sexual stimulation. Couples should allow plenty of time for sexual expression with sufficient foreplay to develop the fullest possible sexual arousal. For some couples, early morning may be a good restful time for sexual expression. Conditions that facilitate sexual pleasure should be explored and may include relaxation, dreams, fantasy, deep breathing, and recalling positive experiences with the partner.

Erection problems are the most common sexual dysfunction for which men seek help after cancer treatment. Many men with erectile dysfunction are able to have an orgasm with oral or manual stimulation; many partners are satisfied and orgasmic with noncoital stimulation. If the desire for intercourse remains, there are several treatment options available for erectile dysfunction depending on the cause and degree of dysfunction. Only a small percentage of men with erection problems seek help.[7,8] With the advent of sildenafil (Viagra), a phosphodiesterase-5 (PDE-5) inhibitor to treat erection problems,[9] the percentage of men who enter into the treatment system for erection problems has increased. Despite the publicity about the effectiveness of sildenafil, it works best in men with the mildest forms of erectile dysfunction. Many men will not be able to achieve adequate erections by taking this drug alone. Sildenafil use allows about 72% of patients with nerve-sparing prostatectomy and 15% of patients with non–nerve-sparing prostatectomy to achieve vaginal intercourse.[10] About 12% of sildenafil responders lose efficacy by 3 years.[11] In a study of brachytherapy in the treatment of localized prostate cancer, sildenafil improved potency in 62% to 70%.[12] Patients who were not being treated with androgen therapy had a significantly better response.[13] Similarly, of men who became impotent after brachytherapy for prostate cancer,[14] 85% to 88% responded with improved erectile function when taking sildenafil. Reported potency rates after prostate brachytherapy are high; a 3-year follow-up study demonstrated that 80% of patients were able to have adequate erections for satisfactory sexual activity with or without siladenafil.[15] Sildenafil has also improved erectile function for patients with partial parasympathetic nerve disruption from rectal surgery.[16,17] No other treatment for erectile dysfunction has a high rate of patient acceptance. Sildenafil has been studied in a novel primary prevention modality using nightly administration after a bilateral nerve-sparing prostatectomy. This approach effected a sevenfold improvement in return of spontaneous, normal erectile function 2 months after discontinuation of the drug.[18] The authors state that this effect appears to be mediated by properties unique to sildenafil that include improved endothelial function and neuronal regeneration and neuroprotection.[18] Published data also suggest that early use of sildenafil after radical retropubic prostatectomy may preserve intracoporeal smooth muscle content;[19] although this effect on the return of potency is not known, maintaining the pro-erectile ultrastructure is integral to rehabilitating post–radical retropubic prostatectomy erectile function.[19] Data on the efficacy of early postoperative erectile treatment rely on very few randomized trials. Larger randomized trials with at least 2 years of follow-up are needed before definitive conclusions can be drawn about the true efficacy of rehabilitative sexual therapy for postoperative erectile function, as the natural recovery of erectile function has been reported to take as long as 2 years.[20]

Currently, there are three U.S. Food and Drug Administration (FDA)–approved PDE-5 inhibitors on the market: Viagra (sildenafil), Levitra (vardenafil), and Cialis (tadalafil). Although all three of these oral medications are PDE-5 inhibitors, they are not the same. No head-to-head comparison trials have been published. It appears, however, that all three agents are similar in efficacy, helping 60% to 70% of patients with erectile dysfunction.[21-23] However, comparisons of the efficacy of the PDE-5 inhibitors are complicated by the heterogeneity of the populations studied, the varied primary cancer therapies employed, different timing in measuring outcomes in the clinical trials, and variance in the endpoints used to determine efficacy. Furthermore, most of these trials were industry sponsored.

The major contraindications for use of a PDE-5 inhibitor are concurrent use of nitrates or the alpha-blockers terazosin (Hytrin) and doxazosin (Cardura). The major difference in the three approved inhibitors is that tadalafil has a considerably longer serum half-life, which provides both a larger window of opportunity and potential side effects.[21,22] There is far more research on the use of sildenafil than on the use of the other PDE-5 inhibitors in oncology patients, as it was approved in 1998; vardenafil and tadalafil were approved in 2003. Tadalafil was investigated in the treatment of erectile dysfunction following bilateral nerve-sparing radical retropubic prostatectomy. Results from this randomized, double-blind, placebo-controlled, multicenter study found that 71% of patients randomly assigned to receive tadalafil reported improved erections.[24] Vardenafil had been investigated in the treatment of erectile dysfunction after radical retropubic prostatectomy and following nerve-sparing radical prostatectomy.[25,26] In post–radical retropubic prostatectomy patients, the average intercourse success rate per patient receiving 20 mg of vardenafil was 74% in men with mild to moderate erectile dysfunction and 28% in men with severe erectile dysfunction, compared with 49% and 4% for placebo.[25] Patients receiving 10-mg and 20-mg doses of vardenafil following nerve-sparing radical prostatectomy reported significantly greater intercourse satisfaction, orgasmic function, and overall satisfaction rate with hardness on the International Index of Erectile Function (IIEF), compared with those receiving placebo.[26]

Therapies such as penile injections, vacuum devices, or intraurethral medication have extremely high dropout rates, and of men who seek help at clinics for erectile dysfunction, only about one third feel long-term satisfaction, despite trying a mean of two different treatment modalities.[27-30] For men who have a suboptimal response to oral therapies after radical retropubic prostatectomy, the use of combined intracorporal injection (ICI) and a PDE-5 inhibitor has been shown to improve erectile function. One retrospective study found that among men who experienced erectile dysfunction after nerve-sparing retropubic prostatectomy, 68% who combined ICI with either sildenafil or vardenafil reported improved erectile function. On follow-up, 36% of these patients used ICI therapy only intermittently, as they reportedly felt that this was adequate for good results.[31]

Rates of long-term satisfaction are superior for penile prosthesis surgery,[32-34] but with less invasive and permanent treatments available, fewer men choose this treatment modality, particularly after undergoing intensive cancer therapy.[35] The role of the man’s partner in prompting him to try a treatment or to keep on using it is also poorly understood. When erectile functioning is impaired, counseling should initially focus on obtaining sexual pleasure and satisfaction without erections or intercourse. For men with postsurgical erectile dysfunction, there is the possibility for improved function over time as nerves may potentially regenerate for up to 2.5 years after surgery.[6] Providers should educate patients that opting to use no medical intervention to restore erections is also a valid choice. Comprehensive reviews of the current management of erectile dysfunction are available.[36-40] Also, several authors [37,41,42] provide further discussion on the management of inhibited sexual desire and other male sexual dysfunctions.

When women experience changes in arousal, most notably vaginal dryness and irritation, vaginal moisturizers (e.g., Replens) and water-based lubricants (e.g., Astroglide and K-Y Liquid) should be suggested, especially in women who cannot use estrogen replacement. The approval of the estradiol-releasing vaginal ring (Estring), containing a slow-release preparation, 2 mg of micronized 17-beta-estradiol, may also provide a less risky alternative to systemic estrogen replacement for women with postmenopausal vaginal atrophy.[43,44] Estring has demonstrated a decreased recurrence of urinary tract infections in postmenopausal women and a significant maturing effect on vaginal and urethral mucosal cells, decreasing the urogenital symptoms of postmenopausal women.[45] Another alternative to local estrogen replacement is the first-available 25-μg 17-beta-estradiol vaginal tablet (Vagifem). A recent study comparing Vagifem tablets to 1.25-mg conjugated equine estrogen vaginal cream (Premarin) found both to be equivalent in relieving symptoms of atrophic vaginitis, with patients who received Vagifem experiencing less endometrial proliferation or hyperplasia. This study also found that women rated vaginal tablets more favorably than vaginal cream.[46]

If changes in arousal are also associated with the endocrine changes of menopause, the option and evaluation of hormone replacement should be discussed. Some women may experience discomfort with penetration around the vaginal entrance and can learn to relax the pubococcygeus muscles with Kegel exercises.[36,47,48] Women who have lost vaginal depth or caliber as a result of pelvic surgery, radiation therapy, or graft-versus-host disease may also benefit from a program of inserting vaginal dilators of gradually increasing sizes, and at the same time, learning exercises to better relax the muscles surrounding the vaginal entrance.[36,49] Some women may also benefit, at least in the short term after cancer treatment, from lubricant or anesthetic gels to prevent pain in tender, dry vulvar areas.[50] The FDA approved a nonpharmaceutical device to aid sexual arousal in women. The EROS clitoral therapy device (EROS-CTD) creates a gentle suction over the clitoris to increase blood flow and sensation. This device is only available by prescription and is clinically indicated for the treatment of female sexual dysfunction. It is expected to be particularly effective in postmenopausal women, women who have had hysterectomies, and those women who have surgically induced menopause.[51] The efficacy of EROS therapy has been supported by several small pilot studies,[52-54] one of which specifically examined its efficacy in alleviating the symptoms of sexual dysfunction among women with a history of irradiated cervical cancer.[53] Three months posttherapy, this study found statistically significant improvements in all domains evaluated, which included increased sexual desire, arousal, lubrication, orgasm, sexual satisfaction, and reduced pain. Additionally, follow-up gynecological examinations revealed improved vaginal elasticity, mucosal color, and moisture and decreased bleeding and ulceration. Randomized controlled trials are warranted to fully assess the benefits of EROS therapy.

More specific information for the evaluation and treatment of female sexual dysfunction, including painful intercourse (i.e., dyspareunia), vaginismus, inhibited orgasm, and sexual arousal and desire disorders, is available in other resources.[37,47,55,56]

For both men and women, a persistent and complex sexual problem is loss of desire for sex after cancer treatment. In men who have not had prostate cancer and have clinically low levels of serum testosterone, replacement by injection or patch is often effective in restoring normal sexual function. Testosterone replacement tends to have little effect, however, if given to a man whose own hormone levels fall within the normal range. Safety, dosage, and delivery systems for androgen replacement in women need to be studied. Media reports have advocated widespread androgen supplementation for women with ovarian failure,[57] yet little is known about the minimum levels of androgens necessary for female sexual function. In a crossover study of transdermal testosterone in premenopausal but otherwise healthy women who had impaired sexual function after oophorectomy and hysterectomy, subjects receiving 300 μg of testosterone per day reported increases in frequency of sexual activity and pleasure.[58] Mood and general well-being also improved during treatment. Two studies have examined the safety and efficacy of a testosterone patch for the treatment of hypoactive sexual desire disorder in surgically menopausal women who did not have breast cancer or gynecologic cancer.[59,60] Data from both of these randomized placebo-controlled trials found that after 24 weeks, women receiving a 300-µg/d testosterone patch had significantly greater increases from baseline in sexual desire and frequency of satisfying sexual activity. For women who have breast cancer, the safety of giving androgens is unknown. Serum androgens can be aromatized to estrogen. Evidence from studies of women who underwent oophorectomy at young ages, showing a reduced long-term risk of breast cancer, may indicate that androgens are a risk factor.[61] Another troubling line of evidence comes from epidemiologic studies suggesting that high androgen levels are present in a subgroup of young women who develop premenopausal breast cancer.[62]

Because loss of desire often is multifactorial, an approach that includes psychological assessment and treatment is usually optimal. An experienced mental health professional can rule out a mood disorder as a factor in loss of desire and can explore the interactions of factors such as changes in relationship dynamics, loss of physical well-being, changes in sexual self-concept, and negative body image. The effects of prescription medications, chemical dependency, or hormonal abnormalities can be recognized and targeted for change. Unfortunately, there is no true aphrodisiac medication that can restore sexual desire in the presence of a normal hormonal environment.

In general, a variety of treatment modalities are available for sexual dysfunction after cancer. For many problems, providing information and suggestions for behavior change in a self-help format may be sufficient. Education can be provided via books,[36] pamphlets,[3,4] CD-ROMs, videos, peer counselors,[63] or Internet interactions. For men and women with more complex and severe problems, professional intervention will be more effective. Future research needs to explore which treatment components are most effective with particular groups of patients. Sexual counseling can be provided for individuals, couples, or groups. The effectiveness of these different formats has not been compared for people with cancer. It is also not known whether brief counseling can enhance the impact of medical treatments, such as those used to overcome erectile dysfunction or dyspareunia. There is limited research about the impact of support groups on sexual outcomes for men with prostate cancer. It is likely that associations between better outcomes and participation in support groups reflect baseline sociographic and clinical differences between those who participate in support groups and those who do not.[64]

References

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  46. Rioux JE, Devlin C, Gelfand MM, et al.: 17beta-estradiol vaginal tablet versus conjugated equine estrogen vaginal cream to relieve menopausal atrophic vaginitis. Menopause 7 (3): 156-61, 2000 May-Jun.  [PUBMED Abstract]

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  49. Parkinson N, Pratt H: Clinical nurse specialists and the psychosexual needs of patients with gynaecological cancer. J Br Menopause Soc 11 (1): 33-5, 2005.  [PUBMED Abstract]

  50. Ganz PA, Greendale GA, Petersen L, et al.: Managing menopausal symptoms in breast cancer survivors: results of a randomized controlled trial. J Natl Cancer Inst 92 (13): 1054-64, 2000.  [PUBMED Abstract]

  51. Josefson D: FDA approves device for female sexual dysfunction. BMJ 320 (7247): 1427, 2000.  [PUBMED Abstract]

  52. Munarriz R, Maitland S, Garcia SP, et al.: A prospective duplex Doppler ultrasonographic study in women with sexual arousal disorder to objectively assess genital engorgement induced by EROS therapy. J Sex Marital Ther 29 (Suppl 1): 85-94, 2003.  [PUBMED Abstract]

  53. Schroder M, Mell LK, Hurteau JA, et al.: Clitoral therapy device for treatment of sexual dysfunction in irradiated cervical cancer patients. Int J Radiat Oncol Biol Phys 61 (4): 1078-86, 2005.  [PUBMED Abstract]

  54. Wilson SK, Delk JR 2nd, Billups KL: Treating symptoms of female sexual arousal disorder with the Eros-Clitoral Therapy Device. J Gend Specif Med 4 (2): 54-8, 2001.  [PUBMED Abstract]

  55. Kaplan HS: The Sexual Desire Disorders. New York, NY: Brunner/Mazel, Inc, 1995. 

  56. Whipple B, McGreer KB: Management of female sexual dysfunction. In: Sipski ML, Alexander CJ, eds.: Sexual Function in People With Disability and Chronic Illness. Gaithersburg, Md: Aspen Publishers, Inc, 1997, pp 511-536. 

  57. Kaplan HS, Owett T: The female androgen deficiency syndrome. J Sex Marital Ther 19 (1): 3-24, 1993 Spring.  [PUBMED Abstract]

  58. Shifren JL, Braunstein GD, Simon JA, et al.: Transdermal testosterone treatment in women with impaired sexual function after oophorectomy. N Engl J Med 343 (10): 682-8, 2000.  [PUBMED Abstract]

  59. Braunstein GD, Sundwall DA, Katz M, et al.: Safety and efficacy of a testosterone patch for the treatment of hypoactive sexual desire disorder in surgically menopausal women: a randomized, placebo-controlled trial. Arch Intern Med 165 (14): 1582-9, 2005.  [PUBMED Abstract]

  60. Buster JE, Kingsberg SA, Aguirre O, et al.: Testosterone patch for low sexual desire in surgically menopausal women: a randomized trial. Obstet Gynecol 105 (5 Pt 1): 944-52, 2005.  [PUBMED Abstract]

  61. Inskip PD: Pelvic radiotherapy, sex hormones, and breast cancer. Cancer Causes Control 5 (5): 471-8, 1994.  [PUBMED Abstract]

  62. Zumoff B: Hormonal profiles in women with breast cancer. Obstet Gynecol Clin North Am 21 (4): 751-72, 1994.  [PUBMED Abstract]

  63. Schover LR, Jenkins R, Sui D, et al.: Randomized trial of peer counseling on reproductive health in African American breast cancer survivors. J Clin Oncol 24 (10): 1620-6, 2006.  [PUBMED Abstract]

  64. Katz D, Koppie TM, Wu D, et al.: Sociodemographic characteristics and health related quality of life in men attending prostate cancer support groups. J Urol 168 (5): 2092-6, 2002.  [PUBMED Abstract]

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